Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome - Shiu, Tzu-Yue; Huang, Hsin-Hung; Lin, Hsuan-Hwai; Shih, Yu-Lueng; Chu, Heng-Cheng; Chang, Wei-Kuo; Hsieh, Tsai-Yuan (Liver international, 2015)
Keywords: Asian Continental Ancestry Group - genetics; Child; Cohort Studies; exon; Exons - genetics; Female; Genetic Predisposition to Disease - epidemiology; Genotype; Gilbert Disease - diagnosis; Gilbert Disease - epidemiology; Gilbert Disease - genetics; Gilbert's syndrome; Glucuronosyltransferase - genetics; Humans; Incidence; Male; Mutation; Polymorphism, Restriction Fragment Length - genetics; Promoter Regions, Genetic - genetics; restriction fragment length polymorphism; Retrospective Studies; Taiwan - epidemiology; UDP-glucuronosyltransferase 1A1; Taiwan; mutation; restriction fragment length polymorphism; Gilbert's syndrome; exon; UDP-glucuronosyltransferase 1A1